Medical Management of Hereditary Optic Neuropathies
Author:
Publisher
Frontiers Media SA
Subject
Clinical Neurology,Neurology
Reference80 articles.
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3. OPA1 mutations induce mitochondrial DNA instability and optic atrophy “plus†phenotypes;Amati-Bonneau;Brain,2008
4. The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS;Pulkes;Ann Neurol,1999
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1. Case report: Mutations in DNAJC30 causing autosomal recessive Leber hereditary optic neuropathy are common amongst Eastern European individuals;Frontiers in Neurology;2023-12-01
2. Idebenone Treatment in Patients with OPA1-Dominant Optic Atrophy: A Prospective Phase 2 Trial;Neuro-Ophthalmology;2023-09-14
3. Current and Future Landscape in Genetic Therapies for Leber Hereditary Optic Neuropathy;Cells;2023-08-07
4. Anastrozole-mediated modulation of mitochondrial activity by inhibition of mitochondrial permeability transition pore opening: an initial perspective;Journal of Biomolecular Structure and Dynamics;2023-02-23
5. Leber Mitochondrial Optic Neuropathy in Pediatric Females With Focus on Very Early Onset Cases;Journal of Child Neurology;2023-01-19
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